HNK-1 sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan

Mutations in multiple genes required for proper O-mannosylation of α-dystroglycan are causal for congenital/limb-girdle muscular dystrophies and abnormal brain development in mammals. Previously, we and others further elucidated the functional O-mannose glycan structure that is terminated by matrigl...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Glycobiology
Päätekijät: Sheikh, M Osman, Venzke, David, Anderson, Mary E, Yoshida-Moriguchi, Takako, Glushka, John N, Nairn, Alison V, Galizzi, Melina, Moremen, Kelley W, Campbell, Kevin P, Wells, Lance
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2020
Aiheet:
Genetic Disorders of Glycosylation
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7673472/
https://ncbi.nlm.nih.gov/pubmed/32149355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/glycob/cwaa024
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